Altalube

Product NDC: 59390-198
11-digit product format: 593900198
Labeler code: 59390
Product ID: 59390-198_0c0e9c0d-6205-e63b-e063-6294a90ac0d9
Type: HUMAN OTC DRUG
Nonproprietary name: Mineral oil and petrolatum
Dosage form: OINTMENT
Route: OPHTHALMIC
Labeler: Altaire Pharmaceuticals Inc.
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2002-02-01
Substance: MINERAL OIL; PETROLATUM
Active strength: 150; 850 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Altalube
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MINERAL OIL	150 mg/g
PETROLATUM	850 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
T5L8T28FGP	Internal UNII lookup
4T6H12BN9U	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
579996	Internal RxNorm lookup
1088146	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
eb65004c-c3a7-4079-bd75-f2857d30c68a	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59390-198-50	Altalube	1 in 1 CARTON	OINTMENT	1		4
59390-198-50	Altalube	3.5 g in 1 TUBE	OINTMENT	3.5		4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59390-198-50	GM - Gram	59390-198	03cbe75b-f0c3-46ac-ab50-9a6f687181b7	1	2018-10-11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59390-198	ALTALUBE (MINERAL OIL AND PETROLATUM) OINTMENT [ALTAIRE PHARMACEUTICALS INC.]	4	Current NDC, Legacy NDC, 2 package rows	20231214_eb65004c-c3a7-4079-bd75-f2857d30c68a.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 26 · 512 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Vedlube	MINERAL OIL AND WHITE PETROLATUM LUBRICANT EYE OINTMENT	VEDCO INC	55d126fa-7489-4307-824e-b6957e57d4e9	2026-07-31	Warnings	Exact identifier application number: M018
Neutraflush	EYEWASH STATION ADDITIVE CONCENTRATE	Aero Healthcare	1d9ff2ef-9c9b-f367-e063-6294a90afa0e	2026-07-24	Warnings	Exact identifier application number: M018
Droptics Dry Eye Relief	CARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80	Droptics LLC	29d7614b-f4b7-48e2-97c5-d1bff27731d2	2026-07-22	Warnings	Exact identifier application number: M018
GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS	POLYVINYL ALCOHOL, POVIDONE	AmerisourceBergen	ce6852a8-c5e6-403d-a7b4-a2e85d1ebb1f	2026-07-22	Warnings	Exact identifier application number: M018
Eyewash Station Additive Concentrate	CHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOL	Global Equipment Company	bc93a1e8-aa3c-6735-e053-2995a90ad6e8	2026-07-16	Warnings	Exact identifier application number: M018
Revitalize Energizing Eye Drops	NAPHAZOLINE HYDROCHLORIDE ,PROPYLENE GLYCOL	Revitalize Energy Inc.	518aac87-1642-4b2f-bca1-b74d21261eea	2026-07-16	Warnings	Exact identifier application number: M018
Polyvinyl Alcohol	POLYVINYL ALCOHOL	AvPAK	f18b61da-4033-341a-e053-2a95a90a8ebf	2026-07-07	Warnings	Exact identifier application number: M018
Artificial Tears	ARTIFICIAL TEARS	AvPAK	f18bebf2-1936-658f-e053-2a95a90a5012	2026-07-07	Warnings	Exact identifier application number: M018
Retaine CMC	CARBOXYMETHYLCELLULOSE SODIUM	OCuSOFT LLC	a3698c71-0c80-4246-be52-5e7d96f6c540	2026-07-06	Warnings	Exact identifier application number: M018
Eyesaline Eyewash Concentrate	PURIFIED WATER	Protective Industrial Products, Inc.	558e5926-9027-d3f6-e063-6294a90ab121	2026-07-02	Warnings	Exact identifier application number: M018
Fendall 2000 Pure Flow	PURIFIED WATER	Protective Industrial Products, Inc.	55a1d07e-0006-0c75-e063-6394a90a7acc	2026-07-02	Warnings	Exact identifier application number: M018
Fendall 1000 Pure Flow	PURIFIED WATER	Protective Industrial Products, Inc.	55a2f4da-bb1e-8ead-e063-6394a90af72e	2026-07-02	Warnings	Exact identifier application number: M018
Sterile Eyesaline Eyewash	STERILE EYESALINE EYEWASH	Protective Industrial Products, Inc.	55a290e8-8310-8be4-e063-6394a90abdce	2026-07-02	Warnings	Exact identifier application number: M018
Eyesaline Emergency Eyewash	PURIFIED WATER	Protective Industrial Products, Inc.	55a261c2-725d-6765-e063-6294a90a3260	2026-07-02	Warnings	Exact identifier application number: M018
OHTrust Artifical Eyedrop	SODIUM CHLORIDE	Nanoplus Technology Co., Limited	2ea26d96-704b-17bb-e063-6394a90a7e27	2026-07-01	Warnings	Exact identifier application number: M018
Fendall 2000 Pure Flow	PURIFIED WATER	Honeywell Safety Products USA, Inc.	37dead3e-60cb-88ae-e063-6294a90a8f70	2026-06-24	Warnings	Exact identifier application number: M018
Rohto Cool Relief	NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80	The Mentholatum Company	dc8f1ff3-87ae-47ca-815f-5a0e34f8cf30	2026-06-19	Warnings	Exact identifier application number: M018
Rohto Sun and Sport	HYPROMELLOSE, POVIDONE	The Mentholatum Company	8bcc8882-b886-4b55-9bc4-d4b92a41358f	2026-06-19	Warnings	Exact identifier application number: M018
Rohto Dual Light Relief	HYPROMELLOSE, POVIDONE	The Mentholatum Company	1b597f83-d7f1-cf93-e063-6394a90a99f7	2026-06-19	Warnings	Exact identifier application number: M018
Lubricant Eye	CARBOXYMETHYLCELLULOSE SODIUM 0.5%	CARDINAL HEALTH 110, LLC. DBA LEADER	51a2d74f-5ff3-9921-e063-6294a90a345a	2026-06-15	Warnings	Exact identifier application number: M018

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
T5L8T28FGP	MINERAL OIL	8042-47-5	MINERAL OIL
4T6H12BN9U	PETROLATUM	8009-03-8	PETROLATUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1088146	Altalube 15 % / 85 % Ophthalmic Ointment	PSN	eb65004c-c3a7-4079-bd75-f2857d30c68a	4
579996	mineral oil 15 % / petrolatum 85 % Ophthalmic Ointment	PSN	eb65004c-c3a7-4079-bd75-f2857d30c68a	4
1088146	mineral oil 0.15 MG/MG / petrolatum 0.85 MG/MG Ophthalmic Ointment [Altalube]	SBD	eb65004c-c3a7-4079-bd75-f2857d30c68a	4
579996	mineral oil 0.15 MG/MG / petrolatum 0.85 MG/MG Ophthalmic Ointment	SCD	eb65004c-c3a7-4079-bd75-f2857d30c68a	4
1088146	Altalube (mineral oil 15 % / petrolatum, white 85 % ) Ophthalmic Ointment	SY	eb65004c-c3a7-4079-bd75-f2857d30c68a	4
579996	mineral oil 15 % / white petrolatum 85 % Ophthalmic Ointment	SY	eb65004c-c3a7-4079-bd75-f2857d30c68a	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59390-198-50	59390019850	1 TUBE in 1 CARTON (59390-198-50) / 3.5 g in 1 TUBE	1 tube	2002-02-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Altalube Ointment	Altaire Pharmaceuticals Inc. \| Altaire Pharmaceuticals, Inc.	2023-12-09	HUMAN OTC DRUG LABEL	4